chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85785931557859316CT21GENIChomozygous53271484
85786052857860529AC14GENIChomozygous52656823
85786065357860654GA23GENIChomozygous53271485
85786076157860762AG33GENIChomozygous52656825
85786093157860932GA42GENIChomozygous52656827
85786114557861146TTAA21GENICheterozygous53207947
85786114557861146TTAAA21GENICheterozygous53461143
85786160357861604CT31GENIChomozygous52656835
85786201657862017GA36GENIChomozygous52656837
85786215457862155AG48GENIChomozygous53271486
85786267957862680TTTG33GENIChomozygous53271487
85786355857863561CTT---14GENIChomozygous53271488
85786380357863804T-8GENICheterozygous53432368
85786610657866107AC26GENIChomozygous52656847
85786670457866706GT--23GENIChomozygous53461145
85786673957866740TG23GENIChomozygous53271489
85786708657867087AC24GENIChomozygous53271490
85786728257867283C-23GENIChomozygous53271491
85786878257868783AG15GENIChomozygous52656855
85786915557869156AC17GENIChomozygous52656857
85786920757869208TC22GENIChomozygous52656859
85787111757871133GCAGCTGGAGTTCCGG----------------22GENIChomozygous53271493
85787124457871245AATTTTTTT7GENIChomozygous52656863
85787277657872777AG28GENIChomozygous52656865
85787281857872819TC33GENIChomozygous52656867
85787474957874750CT32GENIChomozygous53271494